(1S,2R,5S)-5-methyl-2-(propan-2-yl)cyclohexyl 3-oxobutanoate

95%

Reagent Code: #235743
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CAS Number 59557-05-0

science Other reagents with same CAS 59557-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.3386 g/mol
Formula C₁₄H₂₄O₃
badge Registry Numbers
MDL Number MFCD01656135
thermostat Physical Properties
Boiling Point 323.06 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.98 g/cm3
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of steroid-based drugs and anti-inflammatory agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemical control is critical for biological activity. Commonly employed in the development of fragrance compounds due to its terpene-like backbone, contributing to minty or balsamic notes in perfumery. Also utilized in research settings for exploring ester hydrolysis kinetics and enzyme-catalyzed transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,800.00
(1S,2R,5S)-5-methyl-2-(propan-2-yl)cyclohexyl 3-oxobutanoate
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Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of steroid-based drugs and anti-inflammatory agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemical control is critical for biological activity. Commonly employed in the development of fragrance compounds due to its terpene-like backbone, contributing to minty or balsamic notes in perfumery. Also utilized in research settings for exploring ester hydrolysis kinetics and en
Used primarily as an intermediate in the synthesis of pharmaceuticals, especially in the production of steroid-based drugs and anti-inflammatory agents. Its chiral structure makes it valuable in asymmetric synthesis, where stereochemical control is critical for biological activity. Commonly employed in the development of fragrance compounds due to its terpene-like backbone, contributing to minty or balsamic notes in perfumery. Also utilized in research settings for exploring ester hydrolysis kinetics and enzyme-catalyzed transformations.
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